Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03868631
Other study ID # 01435225
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 15, 2016
Est. completion date April 30, 2017

Study information

Verified date February 2020
Source Point Loma Nazarene University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Soy and whey protein have different concentrations of leucine, an amino acid known to be a particularly potent simulator of muscle protein synthesis. The purpose of this study is to determine whether matching soy and whey protein supplements for leucine content instead of by total protein content would contribute to differences in strength increases and muscle growth in response to 12 wk of resistance training.


Recruitment information / eligibility

Status Completed
Enrollment 61
Est. completion date April 30, 2017
Est. primary completion date April 30, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- non-smoking

- body mass index (BMI) 18.5-24.9

- recreationally active

Exclusion Criteria:

- participated in structured weight training during the previous 12 month

- vegetarian or vegan

- presence of chronic disease

- pregnant, postpartum up to six months, lactating, or intention to become pregnant

- allergy to whey or soy

- changes in body weight more than 10 pounds in the past three months

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Whey protein supplement
19 g whey protein isolate (contains 2 g leucine) was consumed daily by one intervention group.
Soy protein supplement
26 g soy protein isolate (contains 2 g leucine) was consumed daily by the other intervention group.

Locations

Country Name City State
United States Arizona State University Phoenix Arizona

Sponsors (1)

Lead Sponsor Collaborator
Point Loma Nazarene University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Lean Body Mass Change assessed using dual energy x-ray absorptiometry (DEXA) scan for changes in lean body mass (kg) Post-12 week intervention
Primary Muscle Tissue Thickness Change assessed using changes in muscle thickness assessed by ultrasound (cm) Post-12 week intervention
Primary Leg Girth Changes assessed using circumference measurements (cm) Post-12 week intervention
Secondary Change in Peak Torque When Doing Leg Extensions Assessed using an isokinetic dynamometer set at 60 degrees of motion per second (d/s) Post-12 week intervention